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间充质细胞软骨生成受到基底膜基质的刺激,并受到与年龄相关因素的抑制。

Mesenchymal cell chondrogenesis is stimulated by basement membrane matrix and inhibited by age-associated factors.

作者信息

Bradham D M, Passaniti A, Horton W E

机构信息

Laboratory of Biological Chemistry, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.

出版信息

Matrix Biol. 1995 Jul;14(7):561-71. doi: 10.1016/s0945-053x(05)80005-8.

Abstract

During development of the embryonic limb, differentiation of mesenchymal progenitor cells into chondrocytes is regulated by cell shape, extracellular matrix, and growth and differentiation factors. In this study, reconstituted basement membrane (Matrigel) prepared from mouse Englebreth-Holm-Swarm tumor tissue was found to stimulate mesenchymal cell chondrogenesis in vitro and the production of cartilage at ectopic sites in athymic mice. The rate of chondrogenesis of mesenchymal cells from chick limb bud was increased four-fold by the addition of 400 micrograms/ml Matrigel to the media of micromass cultures, and this activity was not blocked by neutralizing antibodies to transforming growth factor-beta (TGF-beta) or fibroblast growth factor (FGF). Mesenchymal cells cultured on Matrigel, but not laminin or collagen type I or IV, formed spheres of condensed cells which stained with Alcian blue. Chick limb-bud mesenchymal cells suspended in Matrigel prepared from tumors grown in C57 mice aged 3, 12, or 26 months formed disks of hyaline cartilage within 2 weeks with wet weights of 59.1 mg, 35.7 mg, and 21.4 mg, indicating that the Matrigel from the old animals was less biologically active. In agreement with the in vivo data, Alcian blue staining of proteoglycan was over two-fold higher in micromass cultures supplemented with the Matrigel from young animals than in cultures treated with the Matrigel from old mice. A high-salt wash preparation of Matrigel from tumors grown in old mice increased the rate of chondrogenesis and cartilage production, suggesting that an inhibitor of chondrogenesis is produced by the old host. Thus, Matrigel contains chondrogenic activity distinct from TGF-beta or FGF. The aged host may produce factors that are inhibitory to mesenchymal cell differentiation and adversely affect cartilage formation and repair.

摘要

在胚胎肢体发育过程中,间充质祖细胞向软骨细胞的分化受细胞形状、细胞外基质以及生长和分化因子的调控。在本研究中,发现从小鼠Englebreth-Holm-Swarm肿瘤组织制备的重组基底膜(基质胶)可在体外刺激间充质细胞软骨形成,并在无胸腺小鼠的异位部位产生软骨。向微团培养物的培养基中添加400微克/毫升基质胶,可使鸡胚肢体芽间充质细胞的软骨形成速率提高四倍,并且这种活性不会被转化生长因子-β(TGF-β)或成纤维细胞生长因子(FGF)的中和抗体所阻断。在基质胶上培养的间充质细胞,而非层粘连蛋白、I型或IV型胶原上培养的间充质细胞,形成了用阿尔新蓝染色的凝聚细胞球。悬浮于从3个月、12个月或26个月龄的C57小鼠体内生长的肿瘤制备的基质胶中的鸡胚肢体芽间充质细胞,在2周内形成了透明软骨盘,湿重分别为59.1毫克、35.7毫克和21.4毫克,表明来自老年动物的基质胶生物活性较低。与体内数据一致,补充来自年轻动物的基质胶的微团培养物中蛋白聚糖的阿尔新蓝染色比用来自老年小鼠的基质胶处理的培养物高出两倍多。用高盐洗涤法制备的来自老年小鼠体内生长的肿瘤的基质胶可提高软骨形成速率和软骨产量,这表明老年宿主会产生软骨形成抑制剂。因此,基质胶含有不同于TGF-β或FGF的软骨形成活性。老年宿主可能产生抑制间充质细胞分化并对软骨形成和修复产生不利影响的因子。

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